EP2605743A2 - Haarpflegezusammensetzung - Google Patents

Haarpflegezusammensetzung

Info

Publication number
EP2605743A2
EP2605743A2 EP11724257.8A EP11724257A EP2605743A2 EP 2605743 A2 EP2605743 A2 EP 2605743A2 EP 11724257 A EP11724257 A EP 11724257A EP 2605743 A2 EP2605743 A2 EP 2605743A2
Authority
EP
European Patent Office
Prior art keywords
oil
composition
hair
weight
silicone
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP11724257.8A
Other languages
English (en)
French (fr)
Other versions
EP2605743B1 (de
Inventor
Katya Ivanova
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43447092&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2605743(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Priority to EP11724257.8A priority Critical patent/EP2605743B1/de
Publication of EP2605743A2 publication Critical patent/EP2605743A2/de
Application granted granted Critical
Publication of EP2605743B1 publication Critical patent/EP2605743B1/de
Revoked legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/31Hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

Definitions

  • the present invention relates to a hair conditioning composition comprising an oil blend.
  • WO 01/95866 discloses a hair oil comprising mineral oil and coconut oil. This disclosure demonstrates that adding mineral oil to coconut oil reduces greasiness and increases penetration of total oil in hair.
  • J. Cosmetic Sci., 56, 283-295 discloses that oils applied on hair leave an oily film and oil makes capillary bridges between hair fibres thus 'adhering' fibres together. With time the thickness of the oil film decreases and the adhesion reduces due to the oil being absorbed by the hair (only penetrating oils show this effects). The adhesion between the fibres and the thick oil film lead to greasy feel and weigh down look.
  • the present invention provides a composition according to claim 1 .
  • the first oily component may be present in the hair oil blends of the invention as a single material or as a blend.
  • the total content of first oily component in the hair oil blends of the invention suitably ranges from 10% to 95%, preferably from 20% to 80%, by weight based on total weight of the composition.
  • Suitable hydrocarbon oils include cyclic hydrocarbons, straight chain aliphatic hydrocarbons (saturated or unsaturated), and branched chain aliphatic
  • hydrocarbons saturated or unsaturated.
  • Straight chain hydrocarbon oils will typically contain from about 6 to about 16 carbon atoms, preferably from about 8 up to about 14 carbon atoms.
  • Branched chain hydrocarbon oils can and typically may contain higher numbers of carbon atoms, e.g. from about 6 up to about 20 carbon atoms, preferably from about 8 up to about 18 carbon atoms.
  • Suitable hydrocarbon oils of the invention will generally have a viscosity at ambient temperature (25 to 30°C) of from 0.0001 to 0.5 Pa.s, preferably from 0.001 to 0.05 Pa.s, more preferably from 0.001 to 0.02 Pa.s as measured by a Carri-Med CSL2 100 controlled stress rheometer, from TA Instruments Inc., New Castle, Delaware (USA).
  • a preferred hydrocarbon oil is light mineral oil.
  • Mineral oils are clear oily liquids obtained from petroleum oil, from which waxes have been removed, and the more volatile fractions removed by distillation. The fraction distilling between 250°C to 300°C is termed mineral oil, and it consists of a mixture of hydrocarbons, in which the number of carbon atoms per hydrocarbon molecule generally ranges from Cio to C 4 o.
  • Mineral oil may be characterised in terms of its viscosity, where light mineral oil is relatively less viscous than heavy mineral oil, and these terms are defined more specifically in the U.S. Pharmacopoeia, 22nd revision, p. 899 (1990).
  • a commercially available example of a suitable light mineral oil for use in the invention is Sirius M40 (carbon chain length C10-C28, mainly C12-C20, viscosity 4.3 x 10 "3 Pa.s), available from Silkolene.
  • the hydrocarbon oil may be present in hair oil blends of the invention as a single material or as a blend.
  • the total content of hydrocarbon oil in hair oil blends of the invention suitably ranges from 5% to 90%, preferably from 20% to 80%, by weight based on total weight of the hair oil blend.
  • the first oily component: hydrocarbon oil weight ratio in compositions of the invention may suitably range from 95:5 to 5:95, preferably from 90:10 to 10:90, most preferably from 80:20 to 20:80.
  • Particularly preferred are blends of [coconut oil and/or sunflower oil and/or almond oil] and light mineral oil, in which the
  • oils and glyceride fatty esters may also be present in combination with the hydrocarbon oils and glyceride fatty esters in hair oil blends of the invention.
  • Suitable additional oily materials include other fatty esters, fatty alcohols and fatty ethers.
  • fatty esters, fatty alcohols and ethers are characterised by having at least 10 carbon atoms, and include esters and ethers with hydrocarbyl chains derived from fatty acids or alcohols, e.g., monocarboxylic acid esters, polyhydric alcohol esters, and di- and tricarboxylic acid esters and ethers, and fatty alcohols with a carbon chain carbon chain length of between 10 and 18, e.g. lauryl alcohol, cetyl alcohol or cetostearyl alcohol.
  • Examples include isopropyl myristate, isopropyl palmitate, cetearyl isononanoate, cetearyl octanoate, diethylene glycol monoethyl ether oleate, dicaprylyl ether, caprylic acid/capric acid propylene glycol diester and mixtures of any of the above.
  • the total content of other oily material in compositions of the invention suitably ranges from 0.01 % to 50%, preferably from 1 .0% to 20%, by weight based on total weight of the hair oil blend.
  • the oil blend is present in the composition at from 0.01 to 10% wt. of the composition, more preferably at from 0.1 to 2% wt.
  • Suitable conditioning surfactants are selected from cationic surfactants, used singly or in admixture. Examples include quaternary ammonium hydroxides or salts thereof, e.g. chlorides. Suitable cationic surfactants for use in hair conditioners of the invention include cetyltrimethylammonium chloride, behenyltrimethylammonium chloride,
  • cetylpyridinium chloride tetramethylammonium chloride, tetraethylammonium chloride, octyltrimethylammonium chloride, dodecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octyldimethylbenzylammonium chloride, decyldimethylbenzylammonium chloride, stearyldimethylbenzylammonium chloride, didodecyldimethylammonium chloride, dioctadecyldimethylamnnoniunn chloride, tallowtrimethylamnnoniunn chloride, cocotrimethylammonium chloride, and the corresponding hydroxides thereof.
  • cationic surfactants include those materials having the CTFA designations Quaternium-5, Quaternium-31 and Quaternium-18. Mixtures of any of the foregoing materials may also be suitable.
  • a particularly useful cationic surfactant for use in hair conditioners of the invention is cetyltrimethylammonium chloride, available commercially, for example as
  • the level of cationic surfactant is preferably from 0.01 to 10%, more preferably 0.05 to 5%, most preferably 0.1 to 2% by weight of the composition.
  • compositions of this invention are preferably dedicated hair conditioning compositions and as so comprise less than 5% wt. anionic surfactant, preferably less than 5% wt. cleansing surfactant, more preferably less than 2% wt. anionic surfactant, preferably less than 2% wt. cleansing surfactant, and most preferably no cleansing surfactant.
  • compositions of this invention may contain any other ingredient normally used in hair conditioning formulations.
  • these other ingredients may include, viscosity modifiers, preservatives, colouring agents, polyols such as glycerine and polypropylene glycol, chelating agents such as EDTA, antioxidants such as BHT (butylhydroxytoluene), vitamin E acetate, fragrances, antimicrobials and sunscreens and lipid soluble ingredients e.g. fatty acids or sterols.
  • these optional ingredients are included individually at a level of up to about 5% by weight of the total composition.
  • the composition comprises a conditioning active selected from fatty alcohols and conditioning silicones.
  • Conditioners of the invention advantageously incorporate a fatty alcohol material.
  • fatty alcohol materials and cationic surfactants in conditioning compositions is believed to be especially advantageous, because this leads to the formation of a lamellar phase, in which the cationic surfactant is dispersed.
  • Representative fatty alcohols comprise from 8 to 22 carbon atoms, more preferably 16 to 20.
  • suitable fatty alcohols include cetyl alcohol, stearyl alcohol and mixtures thereof. The use of these materials is also advantageous in that they contribute to the overall conditioning properties of compositions of the invention.
  • the level of fatty alcohol material in conditioners of the invention is conveniently from 0.01 to 10%, preferably from 0.1 to 5% by weight of the composition.
  • the weight ratio of cationic surfactant to fatty alcohol is suitably from 10:1 to 1 :10, preferably from 4:1 to 1 :8, optimally from 1 :1 to 1 :4.
  • Silicone is a particularly preferred ingredient in hair treatment compositions of the invention.
  • conditioners of the invention will preferably also comprise emulsified particles of silicone, for enhancing conditioning performance.
  • the silicone is insoluble in the aqueous matrix of the composition and so is present in an emulsified form, with the silicone present as dispersed particles.
  • Suitable silicones include polydiorganosiloxanes, in particular
  • compositions of the invention which have the CTFA designation dimethicone.
  • polydimethyl siloxanes having hydroxyl end groups which have the CTFA designation dimethiconol.
  • silicone gums having a slight degree of cross-linking as are described for example in WO 96/31 188. These materials can impart body, volume and stylability to hair, as well as good wet and dry conditioning.
  • the viscosity of the emulsified silicone itself (not the emulsion or the final hair conditioning composition) is typically at least 10,000 est. In general we have found that conditioning performance increases with increased viscosity.
  • the viscosity of the silicone itself is preferably at least 60,000 est, most preferably at least 500,000 est, ideally at least 1 ,000,000 est. Preferably the viscosity does not exceed 10 9 est for ease of formulation.
  • Emulsified silicones for use in conditioners of the invention will typically have an average silicone particle size in the composition of less than 30, preferably less than 20, more preferably less than 10 microns. We have found that reducing the particle size generally improves conditioning performance. Most preferably the average silicone particle size of the emulsified silicone in the composition is less than 2 microns, ideally it ranges from 0.01 to 1 micron. Silicone emulsions having an average silicone particle size of ⁇ 0.15 microns are generally termed microemulsions.
  • Particle size may be measured by means of a laser light scattering technique, using a 2600D Particle Sizer from Malvern Instruments.
  • Suitable silicone emulsions for use in the invention are also commercially available in a pre-emulsified form.
  • Suitable pre-formed emulsions include emulsions DC2-1766, DC2- 1784, and microemulsions DC2-1865 and DC2-1870, all available from Dow Corning. These are all emulsions/microemulsions of dimethiconol.
  • Cross-linked silicone gums are also available in a pre-emulsified form, which is advantageous for ease of formulation.
  • a preferred example is the material available from Dow Corning as DC X2-1787, which is an emulsion of cross-linked dimethiconol gum.
  • a further preferred example is the material available from Dow Corning as DC X2- 1391 , which is a microemulsion of cross-linked dimethiconol gum.
  • a further preferred class of silicones for inclusion in conditioners of the invention are amino functional silicones.
  • amino functional silicone is meant a silicone containing at least one primary, secondary or tertiary amine group, or a
  • Suitable amino functional silicones include:
  • G is selected from H, phenyl, OH or d-s alkyl, e.g. methyl;
  • n and n are numbers such that (m + n) can range from 1 to 2000, preferably from 50 to 150;
  • n is a number from 1 to 2000, preferably from 1 to 10;
  • n is a number from 0 to 1999, preferably from 49 to 149, and
  • R is a monovalent radical of formula -C q H 2q L in which q is a number from 2 to 8 and L is an aminofunctional group selected from the following:
  • R is selected from H, phenyl, benzyl, or a saturated monovalent hydrocarbon radical, e.g. Ci -2 o alkyl, and;
  • A is a halide ion, e.g. chloride or bromide.
  • Suitable amino functional silicones corresponding to the above formula include those polysiloxanes termed “trimethylsilylamodimethicone” as depicted below, and which are sufficiently water insoluble so as to be useful in compositions of the invention:
  • R 1 and R 10 may be the same or different and may be independently selected from H, saturated or unsaturated long or short chain alk(en)yl, branched chain alk(en)yl and Cs-Cs cyclic ring systems;
  • R 2 thru' R 9 may be the same or different and may be independently selected from H, straight or branched chain lower alk(en)yl, and Cs-Cs cyclic ring systems; n is a number within the range of about 60 to about 120, preferably about 80, and
  • X " is preferably acetate, but may instead be for example halide, organic carboxylate, organic sulphonate or the like.
  • Suitable quaternary silicone polymers of this class are described in EP-A-0 530 974.
  • Amino functional silicones suitable for use in conditioners of the invention will typically have a mole % amine functionality in the range of from about 0.1 to about 8.0 mole %, preferably from about 0.1 to about 5.0 mole %, most preferably from about 0.1 to about 2.0 mole %. In general the amine concentration should not exceed about 8.0 mole % since we have found that too high an amine
  • the viscosity of the amino functional silicone is not particularly critical and can suitably range from about 100 to about 500,000 est.
  • amino functional silicones suitable for use in the invention are the aminosilicone oils DC2-8220, DC2-8166, DC2-8466, and DC2-8950-1 14 (all ex Dow Corning), and GE 1 149-75, (ex General Electric Silicones).
  • emulsions of amino functional silicone oils with non ionic and/or cationic surfactant are also suitable.
  • Such pre-formed emulsions will have an average amino functional silicone particle size in the composition of less than 30, preferably less than 20, more preferably less than 10 microns. Again, we have found that reducing the particle size generally improves conditioning performance. Most preferably the average amino functional silicone particle size in the composition is less than 2 microns, ideally it ranges from 0.01 to 1 micron. Silicone emulsions having an average silicone particle size of ⁇ 0.15 microns are generally termed
  • Pre-formed emulsions of amino functional silicone are also available from suppliers of silicone oils such as Dow Corning and General Electric. Specific examples include DC929 Cationic Emulsion, DC939 Cationic Emulsion, and the non-ionic emulsions DC2-7224, DC2-8467, DC2-8177 and DC2-8154 (all ex Dow Corning).
  • a quaternary silicone polymer useful in the present invention is the material K3474, ex Goldschmidt.
  • the total amount of silicone incorporated into compositions of the invention depends on the level of conditioning desired and the material used. A preferred amount is from 0.01 to about 10% by weight of the total composition although these limits are not absolute. The lower limit is determined by the minimum level to achieve conditioning and the upper limit by the maximum level to avoid making the hair and/or skin unacceptably greasy.
  • a total amount of silicone of from 0.3 to 5%, preferably 0.5 to 3%, by weight of the total composition is a suitable level.
  • ingredients may include viscosity modifiers, preservatives, colouring agents, polyols such as glycerine and polypropylene glycol, chelating agents such as EDTA, antioxidants such as vitamin E acetate, fragrances, antimicrobials and sunscreens.
  • viscosity modifiers preservatives, colouring agents, polyols such as glycerine and polypropylene glycol, chelating agents such as EDTA, antioxidants such as vitamin E acetate, fragrances, antimicrobials and sunscreens.
  • compositions of this invention also contain adjuvants suitable for hair care.
  • adjuvants suitable for hair care Generally such ingredients are included individually at a level of up to 2%, preferably up to 1 %, by weight of the total composition.
  • Suitable hair care adjuvants are:
  • amino acids and sugars examples include arginine, cysteine, glutamine, glutamic acid, isoleucine, leucine, methionine, serine and valine, and/or precursors and derivatives thereof.
  • the amino acids may be added singly, in mixtures, or in the form of peptides, e.g. di- and tripeptides.
  • the amino acids may also be added in the form of a protein hydrolysate, such as a keratin or collagen hydrolysate.
  • Suitable sugars are glucose, dextrose and fructose. These may be added singly or in the form of, e.g. fruit extracts.
  • hair fibre benefit agents are: ceramides, for moisturising the fibre and maintaining cuticle integrity. Ceramides are available by extraction from natural sources, or as synthetic ceramides and pseudoceramides. A preferred ceramide is Ceramide II, ex Quest. Mixtures of ceramides may also be suitable, such as Ceramides LS, ex Laboratoires Serobi unanimouss. - free fatty acids, for cuticle repair and damage prevention.
  • Examples are branched chain fatty acids such as 18-methyleicosanoic acid and other homologues of this series, straight chain fatty acids such as stearic, myristic and palmitic acids, and unsaturated fatty acids such as oleic acid, linoleic acid, linolenic acid and arachidonic acid.
  • a preferred fatty acid is oleic acid.
  • the fatty acids may be added singly, as mixtures, or in the form of blends derived from extracts of, e.g. lanolin.
  • the composition is a rinse-off conditioning composition.
  • Formulation 1 is inventive formulation while formulations A and B are comparative formulations.
  • Formulation 1 also wins against A and B on the two top boxes which means that the highest percentage of consumers ticking the top two boxes (i.e. 4 and 5) was highest for Example 1 over A and B.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Cosmetics (AREA)
EP11724257.8A 2010-08-20 2011-06-10 Haarpflegezusammensetzung Revoked EP2605743B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11724257.8A EP2605743B1 (de) 2010-08-20 2011-06-10 Haarpflegezusammensetzung

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10173505 2010-08-20
EP11724257.8A EP2605743B1 (de) 2010-08-20 2011-06-10 Haarpflegezusammensetzung
PCT/EP2011/059727 WO2012022516A2 (en) 2010-08-20 2011-06-10 Composition

Publications (2)

Publication Number Publication Date
EP2605743A2 true EP2605743A2 (de) 2013-06-26
EP2605743B1 EP2605743B1 (de) 2015-05-20

Family

ID=43447092

Family Applications (1)

Application Number Title Priority Date Filing Date
EP11724257.8A Revoked EP2605743B1 (de) 2010-08-20 2011-06-10 Haarpflegezusammensetzung

Country Status (10)

Country Link
US (1) US20130189213A1 (de)
EP (1) EP2605743B1 (de)
JP (1) JP2013534230A (de)
CN (1) CN103068361A (de)
BR (1) BR112013001852A2 (de)
EA (1) EA023027B9 (de)
MX (1) MX2013002047A (de)
TW (1) TWI515018B (de)
WO (1) WO2012022516A2 (de)
ZA (1) ZA201300571B (de)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022005811A1 (en) * 2020-06-29 2022-01-06 L'oreal Aerosolized compositions, systems, kits, and methods for keratinous substrates
FR3113459A1 (fr) * 2020-08-18 2022-02-25 L'oreal Compositions aerosolisees, systemes, necessaires, et procedes pour substrats keratineux

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10449132B2 (en) * 2013-09-16 2019-10-22 Kao Corporation Process for treating hair
EP3154641A1 (de) * 2014-06-16 2017-04-19 The Procter & Gamble Company Verfahren zur haarbehandlung mit einer konzentrierten spülung

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH272709A (fr) * 1950-08-22 1950-12-31 Tempia Caliera Pierre Produit pour les soins des poils.
ZA704431B (en) 1969-07-28 1972-02-23 Colgate Palmolive Co Hair conditioning shampoo
GB9116871D0 (en) * 1991-08-05 1991-09-18 Unilever Plc Hair care composition
GB9507130D0 (en) 1995-04-06 1995-05-31 Unilever Plc Hair treatment composition
CN1200023A (zh) * 1995-09-01 1998-11-25 普罗克特和甘保尔公司 含有有机油的头发定型香波
US5935561A (en) * 1996-03-27 1999-08-10 Procter & Gamble Company Conditioning shampoo compositions containing select hair conditioning agents
US6235275B1 (en) * 1999-06-25 2001-05-22 Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. Water-in-oil hair conditioner with lamellar dispersion in water phase
GB0014426D0 (en) * 2000-06-13 2000-08-09 Unilever Plc Hair oils
US6939537B2 (en) * 2001-03-12 2005-09-06 San-Ei Kagaku Co., Ltd. Composition for blending to hair treating agents and a hair treating agent
GB0210936D0 (en) * 2002-05-13 2002-06-19 Unilever Plc Hair conditioning compositions
US20050069508A1 (en) * 2003-08-06 2005-03-31 Karl Pays Cosmetic composition comprising a dispersion of at least one wax in at least one volatile oil
US20050069516A1 (en) * 2003-09-30 2005-03-31 Sidney Hornby Hair conditioning products
US8709453B2 (en) 2004-06-21 2014-04-29 Daniel S. Cap Cosmetic product including vegetable oil blend
FR2873573B1 (fr) 2004-08-02 2006-11-17 Oreal Emulsion eau-dans-huile comprenant une huile non-volatile non-siliconee, un tensioactif cationique, une polyolefine a partie's) polaire(s), et un alkylmonoglycoside ou alkylpolyglycoside
FR2878421B1 (fr) * 2004-11-29 2008-10-31 Michel Aude Barbecue a double foyers verticaux securise
US20060127345A1 (en) * 2004-12-10 2006-06-15 Hilvert Jennifer E Conditioning shampoo containing stabilized silicone particles
US8404218B2 (en) * 2004-12-23 2013-03-26 Conopco, Inc. Gelled water-in-oil microemulsions for hair treatment
US20090098078A1 (en) * 2004-12-23 2009-04-16 Kelvin Brian Dickinson Water-In-Oil Microemulsions for Hair Treatment
EP1827297A1 (de) * 2004-12-23 2007-09-05 Unilever Plc Wasser-in-öl-emulsionen für die haarbehandlung
JP2008525333A (ja) * 2004-12-23 2008-07-17 ユニリーバー・ナームローゼ・ベンノートシヤープ 毛髪トリートメント用油中水型マイクロエマルジョン
WO2006087078A1 (de) * 2005-02-17 2006-08-24 Henkel Kommanditgesellschaft Auf Aktien Kationische shampoo-zusammensetzungen
ATE498428T1 (de) * 2006-07-07 2011-03-15 Unilever Nv Haarkonditionierungszusammensetzungen gegen schuppen
JP5189807B2 (ja) * 2006-08-23 2013-04-24 花王株式会社 水性毛髪化粧料
TWI418368B (zh) 2006-08-23 2013-12-11 Kao Corp 水性毛髮化粧料
JP5648260B2 (ja) * 2007-08-02 2015-01-07 山栄化学株式会社 アルギン酸オリゴ糖(塩)含有毛髪化粧料
BRPI1015471A2 (pt) 2009-04-14 2016-04-26 Alberto Culver Co ativador de gel relaxante

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2012022516A2 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022005811A1 (en) * 2020-06-29 2022-01-06 L'oreal Aerosolized compositions, systems, kits, and methods for keratinous substrates
FR3113459A1 (fr) * 2020-08-18 2022-02-25 L'oreal Compositions aerosolisees, systemes, necessaires, et procedes pour substrats keratineux

Also Published As

Publication number Publication date
EA201390261A1 (ru) 2013-06-28
TW201208714A (en) 2012-03-01
TWI515018B (zh) 2016-01-01
CN103068361A (zh) 2013-04-24
ZA201300571B (en) 2014-03-26
EP2605743B1 (de) 2015-05-20
BR112013001852A2 (pt) 2016-05-31
EA023027B9 (ru) 2016-09-30
MX2013002047A (es) 2013-03-22
JP2013534230A (ja) 2013-09-02
WO2012022516A2 (en) 2012-02-23
US20130189213A1 (en) 2013-07-25
EA023027B1 (ru) 2016-04-29
WO2012022516A3 (en) 2012-08-30

Similar Documents

Publication Publication Date Title
US9402796B2 (en) Kit comprising a hair conditioning composition and an activator composition
AU739034B2 (en) Hair conditioning compositions
MXPA04011179A (es) Composiciones acondicionadores del cabello.
CN113557006A (zh) 用于毛发的沉积系统
AU2009259418A1 (en) Composition
EP2293768A1 (de) Zusammensetzung
US20090041701A1 (en) Hair care composition
EP2296758B1 (de) Haarspülung mit drei silikonpolymeren
EP2605743B1 (de) Haarpflegezusammensetzung
US20090041713A1 (en) Hair Care Composition
WO2010102891A2 (en) Composition
WO2014005821A2 (en) Premix and composition
US20140314702A1 (en) Composition
WO2021115825A1 (en) Cosmetic composition in the form of an oil-in-water nanoemulsion comprising at least one liquid fatty substance, at least one solid fatty substance and at least one cationic surfactant
WO2013037750A1 (en) Kit
US20090044822A1 (en) Hair care composition
WO2003061614A1 (en) Hair conditioning composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20130117

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20140506

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602011016601

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: A61K0008060000

Ipc: A61K0008310000

GRAJ Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted

Free format text: ORIGINAL CODE: EPIDOSDIGR1

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RIC1 Information provided on ipc code assigned before grant

Ipc: A61K 8/31 20060101AFI20141124BHEP

Ipc: A61K 8/92 20060101ALI20141124BHEP

Ipc: A61Q 5/12 20060101ALI20141124BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20150108

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 727361

Country of ref document: AT

Kind code of ref document: T

Effective date: 20150615

REG Reference to a national code

Ref country code: NL

Ref legal event code: T3

Ref country code: IE

Ref legal event code: FG4D

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 5

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602011016601

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 727361

Country of ref document: AT

Kind code of ref document: T

Effective date: 20150520

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150921

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150820

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150820

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150920

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150821

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602011016601

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RO

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20150520

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

26 Opposition filed

Opponent name: HENKEL AG & CO. KGAA

Effective date: 20160215

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

26 Opposition filed

Opponent name: L'OREAL

Effective date: 20160219

Opponent name: KAO GERMANY GMBH

Effective date: 20160222

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20150610

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20150630

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20150630

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 6

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20110610

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

REG Reference to a national code

Ref country code: DE

Ref legal event code: R064

Ref document number: 602011016601

Country of ref document: DE

Ref country code: DE

Ref legal event code: R103

Ref document number: 602011016601

Country of ref document: DE

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20170620

Year of fee payment: 7

Ref country code: DE

Payment date: 20170621

Year of fee payment: 7

Ref country code: FR

Payment date: 20170621

Year of fee payment: 7

RDAF Communication despatched that patent is revoked

Free format text: ORIGINAL CODE: EPIDOSNREV1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20170620

Year of fee payment: 7

Ref country code: IT

Payment date: 20170627

Year of fee payment: 7

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT REVOKED

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20150610

27W Patent revoked

Effective date: 20170725

GBPR Gb: patent revoked under art. 102 of the ep convention designating the uk as contracting state

Effective date: 20170725

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: TR

Payment date: 20180608

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150520

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT REVOKED